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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173930Generated: November 1, 2026

Water → tert-Butyl 4-formyl-5-methoxy-7-methyl-1H-indole-1-carboxylate

https://huagongshe.com/reaction/2173930

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2,6-LutidineHCID 7937—
ReactantSodium periodateHCID 23667635—
Reactanttert-Butyl 5-methoxy-7-methyl-4-(prop-1-en-1-yl)-1H-indole-1-carboxylateHCID 86701481—
CatalystOsmium TetroxideHCID 30318—
Solvent1,4-DioxaneHCID 31275—
Producttert-Butyl 4-formyl-5-methoxy-7-methyl-1H-indole-1-carboxylateHCID 72191522—

Reaction Steps

tert-Butyl 5-methoxy-7-methyl-4-(prop-1-en-1-yl)-1H-indole-1-carboxylate (0.29 g, 0.97 mmol) was dissolved in dioxane (7.27 mL) and water (2.4 mL) and 2,6-lutidine (0.23 mL, 1.94 mmol) was added followed by osmium tetroxide (0.24 mL, 0.019 mmol) and sodium periodate (0.83 g, 3.88 mmol) at 0° C. The reaction was removed from the ice bath and let stir at room temperature for 1 hour. The reaction was diluted with methylene chloride and water. The organic layer was separated, dried over sodium sulfate and then concentrated. The resulting residue was absorbed onto silica and then purified by silica gel flash chromatography (0-50% ethyl acetate/heptanes) to provide the title compound. MS (ESI+) m/z 290.1 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056874B2
Source datasetuspto-grants-2015_06
ORD IDord-8862e0e36afc4bcdb63eeb26c7eb0a64
Source noteuspto-grants-2015_06